Best Practice & Research Clinical Haematology
Volume 22, Issue 4 , Pages 529-536, December 2009

AML in older patients: Are we making progress?

  • Elihu Estey, MD (Professor of Medicine)

      Affiliations

    • Corresponding Author InformationTel.: +1 206 288 7176; Fax: +1 206 288 1119.

Division of Hematology, Fred Hutchinson Cancer Research Center and University of Washington School of Medicine, 825 Eastlake Ave E Mailstop G3-200, Seattle, WA 9810, USA

Older patients are generally, and arbitrarily, defined as those aged 60 and above. It is important to recognise that the effect of age is modulated by numerous other prognostic factors such as performance status, presence of various co-morbidities, and most importantly, cytogenetics. It is generally acknowledged that survival has not improved in a medically significant fashion for older patients. Nonetheless, there has been some progress. Specific improvements include the availability of new therapies, including reduced intensity allogeneic haematopoietic stem cell transplant; the subdivision of the resistant response category into subcategories, such as complete response with incomplete platelet recovery (CRp); the introduction of selection designs prior to initiating large phase 3 trials; the departure from the view that all older patients are the same and are, for example, necessarily candidates for trials of new drugs; increased awareness of the effect of selection bias; and increased questioning of certain practices, such as the imposition of a neutropenic diet, and recommendations to wear masks or avoid crowds.

Keywords: older, acute myeloid leukaemia, CRp, reduced-intensity transplant, resistance, treatment-induced death

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1521-6926(09)00062-0

doi:10.1016/j.beha.2009.08.007

Best Practice & Research Clinical Haematology
Volume 22, Issue 4 , Pages 529-536, December 2009